PREZCOBIX (darunavir/cobicistat) 800/150 mg immediate release film-coated tablets.

PREZCOBIX PRODUCT INFORMATION NAME OF THE MEDICINE PREZCOBIX (darunavir/cobicistat) 800/150 mg immediate release film-coated tablets. Darunavir The chemical name for darunavir is [(1S,2R)-3-[[(4-aminophenyl)sulfonyl](2- methylpropyl)amino]-2-hydroxy-1-(phenylmethyl)propyl]-carbamic acid (3R,3aS,6aR)- hexahydrofuro[2,3-b]furan-3-yl ester. Darunavir has the following chemical structure: O O O O O N H OH N S O NH 2 C 27H 37N 3O 7S MW 547.66 CAS Registry No: 206361-99-1. Cobicistat The chemical name for cobicistat is 1,3-Thiazol-5-ylmethyl [(2R,5R)-5-{[(2S)-2- [(methyl{[2- (propan-2-yl)-1,3-thiazol-4-yl]methyl}carbamoyl)amino]-4-(morpholin-4-yl)butanoyl]amino}- 1,6-diphenylhexan-2-yl]carbamate. Cobicistat has the following chemical structure: C 40H 53N 7O 5S 2 MW 776.0 CAS Registry No: 1004316-88-4. PREZCOBIX(170125)API CCDS 160919 1

DESCRIPTION Antiviral for systemic use. Darunavir is an inhibitor of Human Immunodeficiency Virus type 1 (HIV-1) protease. Darunavir is isolated as darunavir ethanolate, a pseudo-polymorphic form of darunavir. Darunavir ethanolate is a white to off-white powder that is very slightly soluble in water, sparingly soluble in methanol, slightly soluble in ethanol, and freely soluble in acetone and dichloromethane. Cobicistat is a mechanism-based inhibitor of cytochrome P-450 (CYP) enzymes of the CYP3A family. Cobicistat is a white to pale yellow solid with a solubility of 0.1 mg/ml in water at 20 C. The partition coefficient (log p) for cobicistat is 4.3 and the pka is 6.4. Darunavir and Cobicistat are the active substances in the fixed dose combination tablet regimen PREZCOBIX. PREZCOBIX tablets are available as a fixed dose combination 800/150 mg film coated tablet. Each film-coated tablet contains 800 mg of darunavir (corresponding to 867.28 mg darunavir ethanolate and 150 mg of cobicistat). Inactive ingredients: hypromellose, silicon dioxide, silicified microcrystalline cellulose, crospovidone, magnesium stearate and Opadry II 85F140053 Pink (ARTG No.109886) as the tablet film coating. PHARMACOLOGY Pharmacodynamics Mechanism of action Darunavir: Darunavir is an inhibitor of the dimerization and of the catalytic activity of the HIV-1 protease. It selectively inhibits the cleavage of HIV encoded Gag-Pol polyproteins in virus infected cells, thereby preventing the formation of mature infectious virus particles. Darunavir tightly binds to the HIV-1 protease with a K D of 4.5 x 10-12 M. Darunavir shows resilience to the effects of HIV protease inhibitors Resistance-Associated Mutations (RAMs). Darunavir is not an inhibitor of any of 13 tested human cellular proteases. Cobicistat: Cobicistat is a mechanism-based inhibitor of the CYP3A subfamily. Inhibition of CYP3A-mediated metabolism by cobicistat enhances the systemic exposure of CYP3A substrates, such as darunavir, where bioavailability is limited and half-life is shortened by CYP3A-dependent metabolism. PREZCOBIX(170125)API CCDS 160919 2

Antiviral activity in vitro Darunavir: Darunavir exhibits activity against laboratory strains and clinical isolates of HIV-1 and laboratory strains of HIV-2 in acutely infected T-cell lines, human peripheral blood mononuclear cells and human monocytes/macrophages with median EC 50 values ranging from 1.2 to 8.5 nm (0.7 to 5.0 ng/ml). Darunavir demonstrates antiviral activity in vitro against a broad panel of HIV-1 group M (A, B, C, D, E, F, G) and group O primary isolates with EC 50 values ranging from < 0.1 to 4.3 nm. These EC 50 values are well below the 50% cellular toxicity concentration range of 87 µm to > 100 µm. The EC 50 value of darunavir increases by a median factor of 5.4 in the presence of human serum in vitro. Darunavir showed synergistic antiviral activity when studied in combination with the HIV protease inhibitors amprenavir, nelfinavir, or ritonavir and additive antiviral activity when studied in combination with the protease inhibitors atazanavir, indinavir, lopinavir, saquinavir, or tipranavir, the N(t)RTIs abacavir, didanosine, emtricitabine, lamivudine, stavudine, tenofovir, zalcitabine, or zidovudine, the NNRTIs delavirdine, efavirenz, etravirine, rilpivirine, or nevirapine, and the fusion inhibitor enfuvirtide. No antagonism was observed between darunavir and any of those antiretrovirals. Cobicistat: Cobicistat has no detectable antiviral activity in cell culture against HIV-1 and does not antagonize the antiviral activity of darunavir. Resistance in vitro Darunavir: In vitro selection of darunavir-resistant virus from wildtype HIV-1 was lengthy (> 3 years). The selected viruses were unable to grow in the presence of darunavir concentrations above 400 nm. Viruses selected in these conditions and showing decreased susceptibility to darunavir (range: 23-50-fold) harboured 2 to 4 amino acid substitutions in the protease gene. The decreased susceptibility to darunavir of the emerging viruses in the selection experiment could not be explained by the emergence of these protease mutations. In vitro selection of darunavir-resistant HIV-1 (range: 53-641-fold change [FC] in EC 50 values) from 9 HIV-1 strains harbouring multiple PI RAMs resulted in the overall emergence of 22 mutations in the protease, of which L10F, V32I, L33F, S37N, M46I, I47V, I50V, L63P, A71V and I84V were present in more than 50% of the 9 darunavir-resistant isolates. A minimum of 8 of these darunavir in vitro selected mutations, from which at least 2 were already present in the protease prior to selection, were required in the HIV-1 protease to render a virus resistant (FC > 10) to darunavir. In 1113 clinical isolates resistant to amprenavir, atazanavir, indinavir, lopinavir, nelfinavir, ritonavir, saquinavir and/or tipranavir and in 886 baseline isolates from treatment-experienced patients only the subgroups with > 10 PI RAMs showed a median FC for darunavir > 10. PREZCOBIX(170125)API CCDS 160919 3

Cross-resistance in vitro Cross-resistance has been observed among HIV protease inhibitors. Darunavir has a < 10-fold decreased susceptibility against 90% of 3309 clinical isolates resistant to amprenavir, atazanavir, indinavir, lopinavir, nelfinavir, ritonavir, saquinavir and/or tipranavir showing that viruses resistant to most PIs remain susceptible to darunavir. Seven of the 9 darunavir-resistant viruses selected from PI-resistant viruses had phenotypic data for tipranavir. Six of those showed a FC < 3 for tipranavir, indicative of limited cross-resistance between these 2 protease inhibitors. Cross-resistance between darunavir and the nucleoside/nucleotide reverse transcriptase inhibitors, the non-nucleoside reverse transcriptase inhibitors, the entry inhibitors or the integrase inhibitors, is unlikely because the viral targets for those inhibitors are different. Selection of viral resistance in vivo The resistance profile of PREZCOBIX is driven by darunavir. Cobicistat does not select any HIV resistance mutations, due to its lack of antiviral activity. The resistance profile of PREZCOBIX is supported by the analysis of 24 week data from trial GS-US-216-0130 in treatment-naïve and treatment-experienced patients and two Phase III trials conducted with darunavir/ritonavir in treatment-naïve and treatment-experienced patients, respectively. Selection of viral resistance during PREZCOBIX therapy in vivo In the 24 week analysis of the GS-US-216-0130 trial, no PI or NRTI RAMs developed in the treatment-naïve patients. One treatment-experienced patient developed a DRV RAM. This mutation was not associated with a decreased susceptibility to darunavir. One treatment-experienced patient developed an NRTI RAM, which was not associated with a decreased susceptibility to the NRTIs included in the background regimen. Selection of viral resistance during darunavir/ritonavir 800/100 mg q.d. therapy in vivo In the 192 week analysis of the ARTEMIS trial, the proportion of virologic failures was lower in the group of patients receiving darunavir/ritonavir 800/100 mg q.d. than in patients receiving lopinavir/ritonavir 800/200 mg per day (16.0% vs. 20.5%, respectively). In the virologic failures of the darunavir/ritonavir group, 4 patients with developing PI RAMs were identified. In the virologic failures of the lopinavir/rtv group, 9 patients with developing PI RAMs were identified. None of the developing mutations in the darunavir/ritonavir group or in the lopinavir/rtv group were primary (i.e. major) PI mutations. In 4 virologic failures of the darunavir/ritonavir group and 7 virologic failures of the lopinavir/rtv group, a maximum of 2 developing NRTI RAMs were identified identified The development of the NRTI RAM at position 184 (n=9) was associated with a decreased susceptibility to FTC included in the background regimen. In the 48 week analysis of the ODIN trial the proportion of virologic failures was comparable in the darunavir/ritonavir 800/100 mg q.d. group and the darunavir/ritonavir 600/100 mg b.i.d. group (22.1% vs. 18.2%, respectively). In the virologic failures in the darunavir/ritonavir 800/100 mg q.d. group 7 subjects (12%) with developing PI RAMs were PREZCOBIX(170125)API CCDS 160919 4

identified, compared to 4 subjects (10%) in the darunavir/ritonavir 600/100 mg b.i.d. group. One virologic failure subject in the darunavir/ritonavir 800/100 mg q.d. group developed primary (i.e. major) PI mutations, which included 3 DRV RAMs, resulting in decreased susceptibility to darunavir. All the virologic failures from the darunavir/ritonavir 600/100 mg b.i.d. group retained susceptibility to darunavir. Four (6.7%) and 3 (7.1%) virologic failures developed 1 or 2 NRTI RAMs in the darunavir/ritonavir 800/100 mg q.d. and the darunavir/ritonavir 600/100 mg b.i.d. groups, respectively. In 3 and 2 of these virologic failures in the darunavir/ritonavir 800/100 mg q.d. and the darunavir/ritonavir 600/100 mg b.i.d. groups, respectively, the development of these NRTI RAMs was associated with a decreased susceptibility to a NRTI included in the treatment regimen. Cross-resistance with other HIV protease inhibitors in vivo In the virologic failures of the GS-US-216-130 trial no cross-resistance with other PIs was observed. In the virologic failures of the ARTEMIS trial no cross-resistance with other PIs was observed. Of the viruses isolated from subjects receiving darunavir/ritonavir 800/100 mg q.d. experiencing virologic failure in the ODIN trial, 98% remained susceptible to darunavir after treatment. In the same group of subjects, 96% to 100% that were susceptible at baseline to amprenavir, atazanavir, indinavir, lopinavir, saquinavir or tipranavir remained susceptible to these protease inhibitors after treatment. In the virologic failures receiving darunavir/rtv 600/100 mg b.i.d. no cross-resistance with other PIs was observed. Effects on electrocardiogram The electrocardiographic effects of cobicistat were determined in a study of 48 healthy adult subjects. Cobicistat did not prolong the QTcF interval at doses of 250 mg and 400 mg, providing exposures 2-and 4-fold above the recommended therapeutic dose, respectively. A modest increase in PR interval (+9.6 msec) occurred around C max, 3 to 5 hours after dosing of cobicistat 250 mg. This finding was not considered to be clinically significant. Effects on serum creatinine The effect of cobicistat on serum creatinine was investigated in a Phase I study in subjects with normal renal function (egfr 80 ml/min, N=18) and mild to moderate renal impairment (egfr 50-79 ml/min, N=12). A statistically significant change of estimated glomerular filtration rate calculated by Cockcroft-Gault method (egfrcg) from baseline was observed after 7 days of treatment with cobicistat 150 mg among subjects with normal renal function (9.9 ± 13.1 ml/min) and mild to moderate renal impairment (11.9 ± 7.0 ml/min). These decreases in egfr CG were reversible after cobicistat was discontinued. The actual glomerular filtration rate, as determined by the clearance of probe drug iohexol, was not altered from baseline following treatment of cobicistat among subjects with normal renal function and mild to moderate renal impairment, indicating cobicistat inhibits tubular secretion of creatinine, reflected as a reduction in egfr CG, without affecting the actual glomerular filtration rate. PREZCOBIX(170125)API CCDS 160919 5

Pharmacokinetics Darunavir steady state exposure was shown to be comparable between PREZCOBIX and darunavir/ritonavir 800/100 mg q.d. in a bioavailability study in fed conditions in healthy subjects. Bioequivalence between PREZCOBIX and darunavir/cobicistat 800/150 mg co-administered as single agents was established under fed and fasted conditions in healthy subjects (TMC114IFD1001). Absorption: The absolute oral bioavailability of darunavir alone is approximately 37%. Darunavir was rapidly absorbed following oral administration of PREZCOBIX in healthy volunteers. The maximum plasma concentration of darunavir in the presence of cobicistat is generally achieved within 3 to 4.5 hours. Following oral administration of PREZCOBIX in healthy volunteers, maximum plasma concentrations of cobicistat were observed 2 to 5 hours post-dose for cobicistat. When administered with food, the relative exposure of darunavir is 1.7-fold higher as compared to intake without food. Therefore, PREZCOBIX should be taken with food. The type of food does not affect exposure to PREZCOBIX. Distribution: Darunavir: Darunavir is approximately 95% bound to plasma proteins. Darunavir binds primarily to plasma alpha-1-acid glycoprotein. Cobicistat: Cobicistat is 97 to 98% bound to human plasma proteins and the mean plasma to blood-drug concentration ratio was approximately 2. Metabolism: Darunavir: In vitro experiments with human liver microsomes indicate that darunavir primarily undergoes oxidative metabolism. Darunavir is extensively metabolised by the hepatic CYP system and almost exclusively by isozyme CYP3A. A 14 C-darunavir trial in healthy volunteers showed that a majority of the radioactivity in plasma after a single 400/100 mg darunavir/ritonavir dose was due to the parent drug. At least 3 oxidative metabolites of darunavir have been identified in humans; all showed activity that was at least 10-fold less than the activity of darunavir against wildtype HIV. Cobicistat: Cobicistat is metabolized by CYP3A and to a minor extent by CYP2D6 enzymes and does not undergo glucuronidation. Elimination: Darunavir: After a 400/100 mg 14 C-darunavir/ritonavir dose, approximately 79.5% and 13.9% of the administered dose of 14 C-darunavir could be retrieved in faeces and urine, respectively. Unchanged darunavir accounted for approximately 41.2% and 7.7% of the administered dose in faeces and urine, respectively. The intravenous clearance of darunavir PREZCOBIX(170125)API CCDS 160919 6

alone (150 mg) and in the presence of low dose ritonavir was 32.8 L/h and 5.9 L/h, respectively. The terminal elimination half-life of darunavir was approximately 11 hours when combined with cobicistat. Cobicistat: Following oral administration of 14 C-cobicistat, 86% and 8.2% of the dose were recovered in faeces and urine, respectively. The median terminal elimination half-life of cobicistat following administration of cobicistat is approximately 3-4 hours. Special Populations: Paediatric The pharmacokinetics of PREZCOBIX in paediatric patients have not been investigated. Elderly Darunavir: Population pharmacokinetic analysis in HIV infected patients showed that darunavir pharmacokinetics are not different in the age range (18 to 75 years) evaluated in HIV infected patients (see PRECAUTIONS). Cobicistat: Pharmacokinetics of cobicistat have not been fully evaluated in the elderly (65 years of age and older). Renal Impairment PREZCOBIX has not been investigated in patients with renal impairment. Darunavir: Results from a mass balance study with 14 C-darunavir/ritonavir showed that approximately 7.7% of the administered dose of darunavir is excreted in the urine as unchanged drug. Although darunavir has not been studied in patients with renal impairment, population pharmacokinetic analysis showed that the pharmacokinetics of darunavir were not significantly affected in HIV infected patients with moderate renal impairment (CrCl between 30-60 ml/min, n=20) (see DOSAGE AND ADMINISTRATION and PRECAUTIONS). Cobicistat: A study of the pharmacokinetics of cobicistat was performed in non-hiv-1 infected subjects with severe renal impairment (estimated creatinine clearance below 30 ml/min). No meaningful differences in cobicistat pharmacokinetics were observed between subjects with severe renal impairment and healthy subjects, consistent with low renal clearance of cobicistat. Hepatic impairment PREZCOBIX has not been investigated in patients with hepatic impairment. Darunavir: Darunavir is primarily metabolised and eliminated by the liver. In a multiple-dose study with darunavir co-administered with ritonavir (600/100 mg) twice daily, it was demonstrated that the steady-state pharmacokinetic parameters of darunavir in subjects with mild (Child-Pugh Class A, n=8) and moderate (Child-Pugh Class B, n=8) hepatic impairment were comparable with those in healthy subjects. The effect of severe hepatic impairment on PREZCOBIX(170125)API CCDS 160919 7

the pharmacokinetics of darunavir has not been studied (see DOSAGE AND ADMINISTRATION and PRECAUTIONS). Cobicistat: Cobicistat is primarily metabolized and eliminated by the liver. A study of the pharmacokinetics of cobicistat was performed in non-hiv-1 infected subjects with moderate hepatic impairment (Child-Pugh Class B). No clinically relevant differences in cobicistat pharmacokinetics were observed between subjects with moderate impairment and healthy subjects. No dosage adjustment of cobicistat is necessary for patients with mild to moderate hepatic impairment. The effect of severe hepatic impairment (Child-Pugh Class C) on the pharmacokinetics of cobicistat has not been studied. Hepatitis B and/or Hepatitis C Virus Co-infection There were insufficient pharmacokinetic data in the clinical trials to determine the effect of hepatitis B and/or C virus infection on the pharmacokinetics of PREZCOBIX. CLINICAL TRIALS The antiretroviral effect of PREZCOBIX is due to the darunavir component. The activity of cobicistat as a pharmacokinetic enhancer to darunavir has been demonstrated in pharmacokinetic studies. In these pharmacokinetic studies, the exposure of darunavir 800 mg boosted with cobicistat 150 mg was consistent with that observed when boosted with ritonavir 100 mg. Darunavir as a component of PREZCOBIX is bioequivalent to darunavir 800 mg once daily in combination with cobicistat 150 mg once daily co-administered as single agents (see PHARMACOLOGY-Pharmacokinetics). The evidence of efficacy of PREZCOBIX once daily is based on the analysis of 24 week data from study GS-US-216-0130 in treatment-naïve and treatment-experienced patients and two Phase III trials ARTEMIS and ODIN conducted with darunavir/ritonavir 800/100 mg q.d. in treatment-naïve and treatment-experienced patients, respectively. Description of clinical study of darunavir/cobicistat 800/150 mg q.d. in adults GS-US-216-0130 is a single arm, open-label, Phase III trial evaluating the pharmacokinetics, safety, tolerability, and efficacy of darunavir with cobicistat in 313 HIV-1 infected adult patients (295 treatment-naïve and 18 treatment-experienced). These patients received darunavir 800 mg once daily in combination with cobicistat 150 mg once daily with an investigator selected background regimen consisting of 2 active NRTIs. HIV-1 infected patients who were eligible for this trial had a screening genotype showing no darunavir RAMs and plasma HIV-1 RNA 1000 copies/ml. Virologic response was defined as confirmed plasma HIV-1 RNA viral load < 50 copies/ml using the TLOVR analysis. The 313 patients in total had a median age of 35 years (range 18-72), 89.1% were male, 59.7% white, 34.5% black, 21.7% hispanic, and 1.3% asian. The mean baseline plasma HIV-1 RNA and the median baseline CD4+ cell count were 4.8 log 10 copies/ml, 370 x 10 6 cells/l (range 6-1473 x 10 6 cells/l) and 4.8 log 10 copies/ml, 107 x 10 6 cells/l (range 5 643 x 10 6 cells/l) for the treatment-naïve and treatment-experienced patients respectively. PREZCOBIX(170125)API CCDS 160919 8

The table below shows the efficacy data of the 24 week analyses from the GS-US-216-0130 trial: Table 1: 24 Weeks Outcomes at Week 24 a HIV-1 RNA < 50 copies/ml mean HIV-1 RNA log change from baseline (log 10 copies/ml) e Virologic Outcome of Randomized Treatment of Trial GS US 216 0130 at GS-US-216-0130 Treatment-Naïve Treatment-Experienced All subjects darunavir/cobicistat darunavir/cobicistat darunavir/cobicistat 800/150 mg q.d. + 800/150 mg q.d. + 800/150 mg q.d. + OBR OBR OBR N=295 N=18 N=313 232 (78.6%) 8 (44.4%) 240 (76.7%) -3.00-2.56-2.98 CD4+ cell count mean change from baseline 145 99 142 a Imputations according to TLOVR analysis Description of clinical studies of darunavir/ritonavir 800/100 mg q.d. in adults Efficacy of darunavir/ritonavir 800/100 mg q.d in treatment-naïve adult patients The evidence of efficacy of darunavir/ritonavir 800/100 mg q.d. is based on the analyses of 192 week data from the randomized, controlled, open label Phase III trial ARTEMIS in antiretroviral treatment-naïve HIV-1 infected patients comparing darunavir/ritonavir 800/100 mg q.d. with lopinavir/ritonavir 800/200 mg per day (given as a twice daily or as a once daily regimen). Both arms used a fixed background regimen consisting of tenofovir disoproxil fumarate 300 mg q.d. (TDF) and emtricitabine 200 mg q.d. (FTC). HIV-1 infected patients who were eligible for this trial had plasma HIV-1 RNA > 5000 copies/ml. Randomizations was stratified by screening plasma viral load and screening CD4+ cell count. Virologic response was defined as a confirmed plasma HIV-1 RNA viral load < 50 copies/ml. Demographics and baseline characteristics were balanced between the darunavir/ritonavir arm and the lopinavir/ritonavir arm. The 343 patients on darunavir/ritonavir 800/100 mg q.d. had a median age of 34 years (range 18-70), 70% were male, 40% white, 23% black, 23% hispanic, and 13% asian. The mean baseline plasma HIV-1 RNA was 4.86 log 10 copies/ml and the median baseline CD4+ cell count was 228 x 10 6 cells/l (range 4 750 x 10 6 cells/l). Table 2 below shows the efficacy data of the 48 week and 192 week analyses from the ARTEMIS trial: PREZCOBIX(170125)API CCDS 160919 9

Table 2: Efficacy data from the ARTEMIS trial (48 week and 192 week analyses) Outcomes darunavir/ ritonavir 800/100 m g q.d. N=343 HIV-1 RNA 287 < 50 copies/ml c (83.7%) HIV-1 RNA 301 < 400 copies/ml c (87.8%) mean HIV-1 RNA log change from baseline (log10 copies/ml) e median CD4+ cell count change from baseline (x 10 6 /l) e ARTEMIS At Week 48 a lopinavir/ Treatment darunavir/ ritonavir difference ritonavir 800/200 (95% CI of 800/100 mg per day difference) mg q.d. N=346 N=343 271 5.3 236 (78.3%) (-0.5; 11.2) d (68.8%) 295 2.5 258 (85.3%) (-2.6; 7.6) b (75.2%) -2.77-2.65-0.11 f (-0.30; 0.07) d At Week 192 b lopinavir/ ritonavir 800/200 m g per day N=346 198 (57.2%) 225 (65.0%) 137 141 258 263 Treatment difference (95% CI of difference) 11.6 (4.4; 18.8) d 10.2 (3.4; 17.0) -2.35-2.03-0.32 f (-0.55; -0.09 ) a Data based on analyses at Week 48 b Data based on analyses at Week 192 c Imputations according to the TLOVR algorithm d Based on normal approximation to the difference in % response e Non-completer is failure imputation: patients who discontinued prematurely are imputed with a change equal to 0 f Difference in means In the 48 week analysis, the virologic response (HIV-1 RNA < 50 copies/ml) for the darunavir/ritonavir arm was 83.7% and for the lopinavir/rtv arm 78.3%. Statistical comparisons between the treatment arms at Week 48 confirmed non-inferiority of darunavir/ritonavir versus lopinavir/rtv (p-value < 0.001) for both ITT (Intent-To-Treat) & OP (On Protocol) population. Analyses of data at 192 weeks of treatment in the ARTEMIS trial demonstrated sustained antiretroviral efficacy and immunological benefit of the darunavir/ritonavir arm. In the 192 week analysis, virologic response (HIV-1 RNA < 50 copies/ml) was 68.8% and 57.2% for the darunavir/ritonavir and lopinavir/ritonavir arm, respectively. Non-inferiority in virologic response was demonstrated (p < 0.001) for both ITT and OP population. Furthermore, statistical superiority of the darunavir/ritonavir arm over the lopinavir/ ritonavir arm was demonstrated (p=0.002) for both ITT and OP population. The virological response (< 50 copies/ml) at 192 weeks by baseline viral load and baseline CD4+ cell count is presented in Table 3 below: PREZCOBIX(170125)API CCDS 160919 10

Table 3: Virologic Response of Randomized Treatment trial ARTEMIS Week 192 N darunavir/ritonavir 800/100 mg q.d. N=343 number of responders at Week 192 n (%) lopinavir/ritonavir 800/200 mg per day N=346 N number of responders at Week 192 n (%) Treatment difference Difference in % response (95% CI of difference in % response) a Baseline plasma viral load (copies/ml) < 100000 226 157 (69.5%) 226 136 (60.2%) 9.3 (0.5; 18.1) 100000 117 79 (67.5%) 120 62 (51.7%) 15.9 (3.5; 28.3) Baseline CD4+ cell count (x 10 6 /L) < 200 141 92 (65.2%) 148 80 (54.1%) 11.2 (-0.1; 22.5) 200 202 144 (71.3%) 198 118 (59.6%) 11.7 (2.4; 21.0) a Based on a normal approximation to the difference in % response Efficacy of darunavir/ritonavir 800/100 mg q.d. in treatment-experienced adult patients The evidence of comparable efficacy of darunavir/ritonavir 800/100 mg q.d. and darunavir/ritonavir 600/100 mg b.i.d. in treatment-experienced patients with no darunavir RAMs is based on the 48 week analysis of the Phase III trial ODIN. ODIN is a randomized, open-label trial comparing darunavir/ritonavir 800/100 mg q.d. to darunavir/ritonavir 600/100 mg b.i.d. in treatment-experienced HIV-1 infected patients with screening genotype resistance testing showing no darunavir RAMs (i.e. V11I, V32I, L33F, I47V, I50V, I54M, I54L, T74P, L76V, I84V, L89V) and a viral load of > 1000 HIV-1 RNA copies/ml. Both arms used an optimized background regimen consisting of 2 NRTIs selected by the investigator. Demographics and baseline characteristics were balanced between the darunavir/ritonavir q.d. arm and the darunavir/ritonavir b.i.d. arm. The 590 patients in total had a median age of 40 years (range 18-77), 64% were male, 36% white, 26% black, 18% hispanic, and 15% asian. The mean baseline plasma HIV-1 RNA was 4.16 log 10 copies/ml and the median baseline CD4+ cell count was 228 x 10 6 cells/l (range 24 1306 x 10 6 cells/l). The table below shows the efficacy data of the 48 week analysis from the ODIN trial: PREZCOBIX(170125)API CCDS 160919 11

Table 4: Virologic Outcome of ODIN Trial at Week 48 Outcomes HIV-1 RNA < 50 copies/ml a mean HIV-1 RNA log change from baseline (log10 copies/ml) e mean CD4+ cell count change from baseline darunavir/ritonavir 800/100 mg q.d. + OBR N=294 ODIN (x 10 6 /L) c OBR=optimized background regimen a Imputations according to the TLOVR algorithm b c d e darunavir/ritonavir 600/100 mg b.i.d. + OBR N=296 Treatment difference (95% CI of difference) 212 (72.1%) 210 (70.9%) 1.2% (-6.1; 8.5) b -1.84-1.80-0.04 d (-0.24; 0.16) 108 112-5 d Based on a normal approximation of the difference in % response Last Observation Carried Forward imputation Difference in means NC=F (-25; 16) In the 48 week analysis, the virologic response defined as a confirmed plasma HIV-1 RNA viral load < 50 copies/ml, was 72.1% for the darunavir/ritonavir q.d. arm and 70.9% for the darunavir/ritonavir b.i.d. arm. Statistical comparisons between the treatment arms at Week 48 confirmed non-inferiority of darunavir/ritonavir q.d. versus darunavir/rtv b.i.d. for both the ITT and OP population (p-value < 0.001). INDICATIONS PREZCOBIX, a fixed dose combination of darunavir and cobicistat, is indicated in combination with other antiretroviral agents for the treatment of adult patients with human immunodeficiency virus-1 (HIV-1) infection in: - Antiretroviral treatment-naive patients - Antiretroviral treatment-experienced patients with no darunavir resistance associated mutations and who have plasma HIV-1 RNA <100,000 copies/ml - Antiretroviral treatment-experienced but HIV protease inhibitor-naive patients for whom HIV-1 genotype testing is unavailable (see DOSAGE AND ADMINISTRATION) CONTRAINDICATIONS Hypersensitivity to darunavir, cobicistat or to any of the excipients. Darunavir and cobicistat are both inhibitors of the cytochrome P450 3A (CYP3A) isoform. PREZCOBIX should not be co-administered with medicinal products that are highly dependent on CYP3A for clearance and for which increased plasma concentrations are associated with serious and/or life threatening events (narrow therapeutic index). These medicinal products include alfuzosin, astemizole, *apixaban, cisapride, colchicine (in patients with renal and/or hepatic impairment), dronedarone, *elbasvir/grazoprevir, lovastatin, *lurasidone, oral midazolam, pimozide, ranolazine, ergot alkaloids (e.g., dihydroergotamine, PREZCOBIX(170125)API CCDS 160919 12

ergotamine, ergonovine and methylergonovine), sildenafil (when used for treatment of pulmonary arterial hypertension), simvastatin, terfenadine, and triazolam and antiarrhythmic drugs (e.g. amiodarone, bepridil, flecainide, systemic lidocaine, quinidine) (see INTERACTIONS WITH OTHER MEDICINES). *Co-administration of PREZCOBIX with CYP3A inducers may lead to lower exposures of darunavir and cobicistat and potential loss of efficacy of darunavir and possible resistance. Patients taking PREZCOBIX should not use products containing *carbamazepine, phenobarbital, phenytoin, rifampin or St. John s wort. PRECAUTIONS Patients should be advised that current antiretroviral therapy does not cure HIV and has not been proven to prevent the transmission of HIV. Appropriate precautions should continue to be employed. Hepatotoxicity Drug induced hepatitis (e.g. acute hepatitis, cytolytic hepatitis) has been reported with darunavir/ritonavir. During the darunavir clinical development program (N=3063), hepatitis was reported in 0.5% of patients receiving combination therapy with darunavir/ritonavir. Patients with pre-existing liver dysfunction, including chronic active hepatitis B or C, have an increased risk for liver function abnormalities including severe hepatic adverse events. Appropriate laboratory testing should be conducted prior to initiating therapy with PREZCOBIX and patients should be monitored during treatment. Increased AST/ALT monitoring should be considered in patients with underlying chronic hepatitis, cirrhosis, or in patients who have pre-treatment elevations of transaminases, especially during the first several months of PREZCOBIX treatment. Evidence of new or worsening liver dysfunction (including clinically significant elevation of liver enzymes and/or symptoms such as fatigue, anorexia, nausea, jaundice, dark urine, liver tenderness, hepatomegaly) in patients on PREZCOBIX should prompt consideration of interruption or discontinuation of treatment. Severe skin reactions During the darunavir clinical development program (N=3063), where darunavir was co-administered with low-dose ritonavir, severe skin reactions, which may be accompanied with fever and/or elevations of transaminases, have been reported in 0.4% of patients. Stevens Johnson Syndrome has been rarely (< 0.1%) reported; and during post-marketing experience toxic epidermal necrolysis, *Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) and acute generalized exanthematous pustulosis have been reported very rarely (< 0.01%). Discontinue PREZCOBIX immediately if signs or symptoms of severe skin reactions develop. These can include but are not limited to severe rash or rash accompanied with fever, general malaise, fatigue, muscle or joint aches, blisters, oral lesions, conjunctivitis, hepatitis and/or eosinophilia. Rash (all severity grades, regardless of causality) occurred in 10.3% of patients treated with darunavir/ritonavir (see Adverse Reactions). Rash was mostly mild-to-moderate, often PREZCOBIX(170125)API CCDS 160919 13

occurring within the first four weeks of treatment and resolving with continued dosing. The discontinuation rate due to rash in patients using darunavir/ritonavir was 0.5%. Rash occurred more commonly in treatment-experienced subjects receiving regimens containing darunavir/ritonavir + raltegravir compared to subjects receiving darunavir/ritonavir without raltegravir or raltegravir without darunavir/ritonavir. However, rash that was considered drug related occurred at similar rates for all three groups. These rashes were mild to moderate in severity and did not limit therapy; there were no discontinuations due to rash. In a single-arm trial investigating darunavir 800 mg once daily in combination with cobicistat 150 mg once daily and other antiretrovirals, 16.0% of patients experienced rash, and 2.2% discontinued treatment due to rash. Rash was mostly mild-to-moderate, often occurring within the first four weeks of treatment and resolving with continued dosing. Darunavir contains a sulfonamide moiety. PREZCOBIX should be used with caution in patients with a known sulfonamide allergy. In clinical studies with darunavir/ritonavir, the incidence and severity of rash was similar in patients with or without a history of sulfonamide allergy. Hemophiliac patients There have been reports of increased bleeding, including spontaneous skin hematomas and hemarthrosis in patients with hemophilia type A and B treated with HIV protease inhibitors (PIs). In some patients additional factor VIII was given. In more than half of the reported cases, treatment with HIV PIs was continued or reintroduced if treatment had been discontinued. A causal relationship has been suggested, although the mechanism of action has not been elucidated. Hemophiliac patients should therefore be made aware of the possibility of increased bleeding. Diabetes mellitus/hyperglycaemia New onset diabetes mellitus, hyperglycemia, or exacerbation of existing diabetes mellitus has been reported in patients receiving antiretroviral therapy, including HIV PIs. In some of these patients the hyperglycemia was severe and in some cases also associated with ketoacidosis. Many patients had confounding medical conditions some of which required therapy with agents that have been associated with the development of diabetes mellitus or hyperglycemia. Fat redistribution & metabolic disorders Combination antiretroviral therapy has been associated with redistribution of body fat (lipodystrophy) in HIV infected patients. The long term consequences of these events are currently unknown. Knowledge about the mechanism is incomplete. A connection between visceral lipomatosis and HIV PIs and lipoatrophy and NRTIs has been hypothesized. A higher risk of lipodystrophy has been associated with individual factors such as older age, and with drug related factors such as longer duration of antiretroviral treatment and associated metabolic disturbances. Clinical examination should include evaluation for physical signs of fat redistribution. Consideration should be given to measurement of fasting PREZCOBIX(170125)API CCDS 160919 14

serum lipids and blood glucose. Lipid disorders should be managed as clinically appropriate (see ADVERSE REACTIONS). Immune reconstitution inflammatory syndrome In HIV infected patients with severe immune deficiency at the time of institution of combination antiretroviral therapy (CART), an inflammatory reaction to asymptomatic or residual opportunistic pathogens may arise and cause serious clinical conditions, or aggravation of symptoms. Typically, such reactions have been observed within the first weeks or months of initiation of CART. Relevant examples are cytomegalovirus retinitis, generalized and/or focal mycobacterial infections, and Pneumocystis jirovecii pneumonia. Any inflammatory symptoms should be evaluated and treatment instituted when necessary. Autoimmune disorders such as Graves disease have also been reported to occur in the setting of immune reconstitution; however, the time to onset is more variable, and can occur many months after initiation of treatment (see ADVERSE REACTIONS). Effects on fertility There was no effect on mating or fertility with darunavir or cobicistat treatment in rats. No effect on mating or fertility is expected with PREZCOBIX. Darunavir: In a study conducted in rats, there were no effects on mating with darunavir treatment up to 1000 mg/kg/day, but exposure levels were below (AUC - 0.5 fold) that in humans at the clinically recommended dose. The number of corporea lutea and hence the number of live young was lower for females at 1000 mg/kg/day darunavir, and correlated with lower maternal body weight; the NOEL for effects on fertility was 200 mg/kg/day darunavir (corresponding to an exposure level 0.3 fold that in humans at the recommended clinical dose). Cobicistat: Cobicistat did not affect fertility in male or female rats at daily exposures (AUC) approximately 4-fold higher than human exposures at the recommended 150 mg daily dose. Fertility was normal in the offspring of rats exposed daily from before birth (in utero) through sexual maturity at daily exposures (AUC) of approximately 1.2-fold higher than human exposures at the recommended 150 mg daily dose. Use in pregnancy Category B2 There are no adequate and well-controlled studies of PREZCOBIX, darunavir, or cobicistat in pregnant women. At clinically relevant exposures of darunavir and cobicistat, animal studies do not indicate direct or indirect harmful effects with respect to developmental or reproductive toxicity. PREZCOBIX should be used during pregnancy only if the potential benefit justifies the potential risk. Use in lactation It is not known whether darunavir, cobicistat or their metabolites are excreted in human milk. Animal studies have demonstrated that darunavir and cobicistat are excreted in milk. Because of both the potential for HIV transmission and the potential for serious adverse events in nursing infants, mothers should be instructed not to breastfeed if they are receiving PREZCOBIX. PREZCOBIX(170125)API CCDS 160919 15

In a pre and postnatal development assessment in rats, darunavir with and without ritonavir, caused a transient reduction in body weight of the offspring during lactation. This was attributed to drug exposure via the milk. No post weaning functions were affected with darunavir alone or in combination with ritonavir. In juvenile rats directly dosed with darunavir (from 20 mg/kg to 1000 mg/kg) up to days 23 to 26 of age, mortality was observed and, in some of the animals, convulsions. Within this age range exposures in plasma, liver and brain were dose and age dependent and were considerably greater than those observed in adult rats. These findings were attributed to the ontogeny of the CYP450 liver enzymes involved in the metabolism of darunavir and the immaturity of the blood brain barrier. No treatment related mortalities were noted in juvenile rats dosed at 1000 mg/kg darunavir (single dose) on day 26 of age or at 500 mg/kg (repeated dose) from day 23 to 50 of age, and the exposures and toxicity profile were comparable to those observed in adult rats. Due to uncertainties regarding the rate of development of the human blood brain barrier and liver enzymes, darunavir /ritonavir should not be used in paediatric patients below 3 years of age. Paediatric use The safety and efficacy of PREZCOBIX in paediatric patients have not been established. Use in the elderly As limited information is available on the use of PREZCOBIX in patients aged 65 and over, caution should be exercised in the administration of PREZCOBIX in elderly patients, reflecting the greater frequency of decreased hepatic function and of concomitant disease or other therapy (see Pharmacokinetics-Elderly). Patients with Co-existing Conditions Patients with hepatic impairment There are no pharmacokinetic data obtained with PREZCOBIX in patients with hepatic impairment. However, there are pharmacokinetic data for the single agents of PREZCOBIX, darunavir and cobicistat. PREZCOBIX should be used with caution in patients with severe hepatic impairment. Data demonstrated that the steady state pharmacokinetic parameters of darunavir co-administered with low-dose ritonavir in subjects with mild and moderate hepatic impairment were comparable with those in healthy subjects. No clinically relevant differences in cobicistat pharmacokinetics were observed between subjects with moderate hepatic impairment (Child-Pugh Class B) and healthy subjects. No dose adjustment for PREZCOBIX is required in patients with mild or moderate hepatic impairment (see PHARMACOLOGY- Special Populations-Hepatic impairment and DOSAGE AND ADMINISTRATION). Patients with renal impairment Since the renal clearance of darunavir and cobicistat is limited, a decrease in total body clearance of darunavir and cobicistat is not expected in patients with renal impairment. As darunavir and cobicistat are highly bound to plasma proteins, it is unlikely that they will be PREZCOBIX(170125)API CCDS 160919 16

significantly removed by hemodialysis or peritoneal dialysis. (see PHARMACOLOGY-Special Populations-Renal impairment and DOSAGE AND ADMINISTRATION). Cobicistat has been shown to decrease estimated creatinine clearance due to inhibition of tubular secretion of creatinine without affecting actual renal glomerular function (see also section PHARMACOLOGY-Pharmacodynamics-Effects on serum creatitinine, and prescribing information for cobicistat). An increase in serum creatinine due to cobicistat's inhibitory effect generally does not exceed 0.4 mg per dl from baseline. This effect should be considered when PREZCOBIX is co-administered with a drug that has dosing adjustment recommendations guided by estimated creatinine clearance. Carcinogenicity Darunavir was evaluated for carcinogenic potential by oral gavage administration to mice and rats up to 104 weeks. Daily doses of 150, 450 and 1000 mg/kg were administered to mice and doses of 50, 150 and 500 mg/kg were administered to rats. Dose-related increases in the incidences of hepatocellular adenomas and carcinomas were observed in males and females of both species. Thyroid follicular cell adenomas were noted in male rats. Administration of darunavir did not cause a statistically significant increase in the incidence of any other benign or malignant neoplasm in mice or rats. The observed hepatocellular findings in rodents are considered to be of limited relevance to humans. Repeated administration of darunavir to rats caused hepatic microsomal enzyme induction and increased thyroid hormone elimination, which predispose rats, but not humans, to thyroid neoplasms. At the highest tested doses, the systemic exposures (based on AUC) to darunavir were between 0.4- and 0.7-fold (mice) and 0.7- and 1-fold (rats), relative to those observed in humans at the recommended therapeutic doses (600/100 mg twice daily or 800/100 mg once daily). Genotoxicity Darunavir was not mutagenic or genotoxic in a battery of in vitro and in vivo assays including bacterial reverse mutation (Ames), chromosomal aberration in human lymphocytes and in vivo micronucleus test in mice. Darunavir: Animal toxicology studies have been conducted with darunavir alone, in mice, rats and dogs and in combination with ritonavir in rats and dogs. In chronic toxicology studies in rats and dogs, there were only limited effects of treatment with darunavir. In the rat the key target organs identified were the haematopoietic system, the blood coagulation system, liver and thyroid, observed at 100 mg/kg/day and above and at exposures below clinical levels. A variable but limited decrease in red blood cell-related parameters was observed, together with increases in activated PTT. The observed liver and thyroid changes were considered to reflect an adaptive response to enzyme induction in the rat rather than an adverse effect. In combination toxicity studies with ritonavir, no additional target organs of toxicity were reported in rats. In the dog, no major toxicity findings or key target organs were identified at doses up to 120 mg/kg/day and exposures equivalent to clinical exposure at the recommended dose. Cobicistat: Cobicistat was not genotoxic in the reverse mutation bacterial test (Ames test), mouse lymphoma or rat micronucleus assays. PREZCOBIX(170125)API CCDS 160919 17

Effects on Laboratory Tests None known. Effect on Ability to Drive or Operate Machinery No trials on the effects of PREZCOBIX, darunavir, or cobicistat on the ability to drive or use machines have been performed. However, dizziness has been reported in some patients during treatment with regimens containing darunavir and should be borne in mind when considering a patient s ability to drive or operate machinery (see ADVERSE EFFECTS). INTERACTIONS WITH OTHER MEDICINES No drug interactions studies have been performed using PREZCOBIX. As PREZCOBIX contains darunavir and cobicistat, interactions that have been identified with darunavir (in combination with low-dose ritonavir) and with cobicistat determine the interactions that may occur with PREZCOBIX. Interaction studies with darunavir/ritonavir and with cobicistat have only been performed in adults. Darunavir and cobicistat are metabolized by CYP3A. Drugs that induce CYP3A activity would be expected to lower plasma concentrations of darunavir and cobicistat, *which could potentially lead to loss of efficacy of darunavir and possible development of resistance (see CONTRAINDICATIONS). Co-administration of PREZCOBIX and other drugs that inhibit CYP3A may increase plasma concentrations of darunavir and cobicistat (see INTERACTIONS WITH OTHER MEDICINES). PREZCOBIX should not be used in combination with another antiretroviral that requires pharmacokinetic boosting. PREZCOBIX should not be used concurrently with products or regimens containing darunavir, ritonavir or cobicistat. Darunavir is an inhibitor of CYP3A, *a weak inhibitor of CYP2D6, and an inhibitor of P-gp. Cobicistat is an inhibitor of CYP3A and CYP2D6. *Cobicistat inhibits the transporters p-glycoprotein (P-gp), BCRP, OATP1B1 and OATP1B3. Cobicistat is not expected to inhibit CYP1A2, CYP2B6, CYP2C8, CYP2C9 or CYP2C19. Cobicistat is not expected to induce CYP1A2, CYP3A4, CYP2C9, CYP2C19, uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1), or multidrug resistance protein 1 (MDR1). Co-administration of PREZCOBIX and medicinal products primarily metabolized by CYP3A *and/or CYP2D6 may result in increased plasma concentrations of such medicinal products, which could increase or prolong their therapeutic effect and can be associated with serious and/or life threatening adverse events (see CONTRAINDICATIONS). *The interaction profile of darunavir depends on whether ritonavir or cobicistat is used as pharmacokinetic enhancer, therefore there may be different recommendations for the use of darunavir with concomitant medicines. In the table below it is specified when recommendations for PREZCOBIX differ from those for darunavir boosted with low dose ritonavir. Refer to the product information for PREZISTA (darunavir) for further information. For additional drug-drug interactions with darunavir or cobicistat, consult their respective Product Information when using PREZCOBIX. PREZCOBIX(170125)API CCDS 160919 18

Table 5: Drug Interactions: Alterations in Dose or Regimen May Be Recommended Based on Drug Interaction Studies or Predicted Interaction Concomitant Drug Class: Drug Name Effect on Concentration of Darunavir, cobicistat or Concomitant Drug Clinical Comment HIV-1-Antiviral Agents: Nucleoside Reverse Transcriptase Inhibitors (NRTIs) didanosine tenofovir disoproxil fumarate Other NRTIs: abacavir, emtricitabine, lamivudine, stavudine, zalcitabine, zidovudine darunavir cobicistat didanosine darunavir cobicistat tenofovir darunavir PREZCOBIX and didanosine can be used without dose adjustments. As it is recommended that didanosine be administered on an empty stomach, didanosine should be administered one hour before or two hours after PREZCOBIX (administered with food). Co-administration of PREZCOBIX with tenofovir disoproxil fumarate may increase concentrations of tenofovir (inhibition of P-glycoprotein). The increase in tenofovir is not expected to be clinically relevant and no dose adjustment of tenofovir disoproxil fumarate is needed. Based on the different elimination pathways of the other NRTIs, which are primarily renally excreted, no drug interactions are expected for these medicinal products and PREZCOBIX HIV-1-Antiviral Agents: Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) delavirdine efavirenz, etravirine, neviraprine rilpivirine darunavir cobicistat delavirdine darunavir cobicistat nevirapine darunavir cobicistat rilpivirine Co-administration of PREZCOBIX and delavirdine may increase darunavir, cobicistat and/or delavirdine concentrations (inhibition of CYP3A). The appropriate doses of PREZCOBIX and delavirdine have not been established. The combination of PREZCOBIX and delavirdine is not recommended. Co-administration of PREZCOBIX with these NNRTIs may decrease darunavir and/or cobicistat concentrations (induction of CYP3A) which may result in loss of therapeutic effect *and development of resistance. Nevirapine concentrations may be increased when coadministered with PREZCOBIX. Co-administration of PREZCOBIX with these NNRTIs is not recommended. *The recommendation is different from ritonavir-boosted darunavir. Consult the local product information for darunavir for further details. Co-administration of PREZCOBIX with rilpivirine may increase concentrations of rilpivirine (inhibition of CYP3A). The increase in rilpivirine is not expected to be clinically relevant and no dose adjustment of rilpivirine is needed when coadministered with PREZCOBIX. PREZCOBIX(170125)API CCDS 160919 19